Variant report

Variant	rs555535786
Chromosome Location	chr1:213084510-213084511
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1008383	chr1:213025546-213114894	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	esv3403224	chr1:213081429-213085627	Active TSS Enhancers Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv3437401	chr1:213082329-213088502	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
4	esv3337955	chr1:213083029-213088127	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	esv3428295	chr1:213083029-213088127	Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	esv1000808	chr1:213083340-213087446	Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Enhancers	n/a	n/a	inside rSNPs	diseases
7	nsv511730	chr1:213083776-213086646	Active TSS Weak transcription	n/a	n/a	inside rSNPs	diseases
8	esv3379052	chr1:213083795-213086533	Active TSS Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:213073800-213089000	Weak transcription	Pancreas	Pancrea
2	chr1:213079600-213090000	Weak transcription	Right Atrium	heart
3	chr1:213081600-213088000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr1:213083200-213084600	Active TSS	ES-I3 Cell Line	embryonic stem cell
5	chr1:213083200-213086400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr1:213083200-213088000	Active TSS	iPS-20b Cell Line	embryonic stem cell
7	chr1:213083200-213089000	Active TSS	H9 Cell Line	embryonic stem cell
8	chr1:213083400-213088000	Active TSS	iPS-18 Cell Line	embryonic stem cell
9	chr1:213084200-213084600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
10	chr1:213084200-213086200	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr1:213084200-213086400	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr1:213084200-213086400	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr1:213084200-213086400	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr1:213084200-213086400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr1:213084200-213086400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr1:213084200-213086400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr1:213084200-213088600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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